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Perovskite and chalcogenide quantum dots (QDs) are important nano semiconductors. It has been a challenge to synthesize heterostructural QDs combining perovskite and chalcogenide with tailorable photoelectronic properties. In this report, heterostructural CsPbX3-PbS (X = Cl, Br, I) QDs were successfully synthesized via a room temperature in situ transformation route. The CsPbX3-PbS QDs show a tunable dual emission feature with the visible and near-infrared (NIR) photoluminescence (PL) corresponding to CsPbX3 and PbS, respectively. Typically, the formation and evolution of the heterostructural CsPbBr3-PbS QDs with reaction time was investigated. Femtosecond transient absorption spectroscopy (TAS) was applied to illuminate the exciton dynamics in CsPbBr3-PbS QDs. The mild synthetic method and TAS proved perovskite to PbS energy transfer may pave the way toward highly efficient QD photovoltaic and optoelectronic devices.pi-stacked organic chromophores are highly tunable light absorbers with many potential applications in optoelectronics. Their optical properties are highly dependent on the nature and energy of electron-hole pairs or excitons formed upon light absorp-tion, which are in turn determined by the intra- and inter-molecular electronic and vibrational excitations. Here, we present a first-principles approach for describing the optical spectrum of stacked organic molecules with strong vibronic coupling. For stacked perylene tetracarboxylic acid diimides, we describe optical excitations within time-dependent density functional theory with a Franck-Condon Herzberg-Teller approximation of vibronic effects and validate our approach with comparison to exper-imental UV-vis absorption measurements of solvated stacks. We determine that for these macromolecules, unlike for single molecules, the sampling of the ground state potential energy surface significantly influence the optical absorption spectrum. We account for this effect by applying our analysis to ~ 100 structures extracted from equilibrated molecular dynamics simula-tions and averaging the optical spectrum over the ensemble when comparing to measurement. Additionally, we demonstrate that inter-molecular electronic coupling within stacks results in multiple low-energy electronically excited states that all con-tribute to the optical spectrum. This study provides a computationally feasible recipe for describing the spectroscopic proper-ties of stacked organic chromophores via first-principles density functional theory.Ammonia cluster cations are a chemical species that has recently attracted considerable research attention as an ion-molecule reaction species in the planetary atmosphere, surface reaction species in materials chemistry, and super-alkali species. Reactions of the radical cation of an ammonia cluster, [(NH3)n]+ (n = 2-6), following the ionization of the parent neutral cluster, were investigated using direct ab initio molecular dynamics to elucidate the reactions of the ammonia cluster cation under astrochemical conditions. The calculations showed that two competing reaction channels-proton transfer (PT) channel and complex formation channel-operate after the ionization of neutral clusters. In the PT channel, a proton of NH3+ was transferred to a neighboring ammonia molecule. The PT channel was found in all clusters (n = 2-6). Reaction via the PT channel became faster with increasing cluster size and saturated around n = 5-6. In the complex formation channel, a face-to-face complex having a H3N-NH3+ structure (with a N-N bond) was formed. This channel was found only in larger clusters (n = 5-6). Time scales of PT and complex formation channels were calculated to be 20-30 and 40-50 fs, respectively. The reaction mechanism was discussed based on the results of theoretical calculations.Glufosinate is considered a contact herbicide because of its fast activity and limited translocation in plants. We used Palmer amaranth (Amaranthus palmeri S. Watson) as a model species to study plant-related factors affecting glufosinate uptake and translocation. Glufosinate uptake increased rapidly during the initial 24 h, achieving maximum uptake from this time on. The rate of uptake saturated with doses higher than 250 μM glufosinate, suggesting the involvement of a membrane transporter. When glufosinate concentrations were higher (>1 mM), uptake was a simple diffusion process in favor of a concentration gradient between the inside and the outside of the cells. Glufosinate uptake was inhibited by the presence of glutamine. The fast action of glufosinate did not limit its own translocation. Because glufosinate is highly water soluble, it translocates mostly through the apoplast or the xylem system. Consequently, old leaves tend to accumulate more herbicide than young meristematic leaves.We describe libmolgrid, a general-purpose library for representing three-dimensional molecules using multidimensional arrays of voxelized molecular data. libmolgrid provides functionality for sampling batches of data suited to machine learning workflows, and it also supports temporal and spatial recurrences over that data to facilitate work with convolutional and recurrent neural networks. It was designed for seamless integration with popular deep learning frameworks and features optimized performance by leveraging graphics processing units (GPUs). libmolgrid is a free and open source project (GPLv2) that aims to democratize grid-based modeling in computational chemistry.Employing isotope incubation studies, the biosynthetic pathway leading to a series of benzylic derivatives was elucidated in the fermentation broth of the edible mushroom Ischnoderma resinosum (P. Karst). Twenty-six hydroxy- and methoxy- benzylic derivatives were screened by gas chromatography-mass spectrometry (GC-MS) of which 13 were detected in the culture media. Results from the isotope incubation studies showed the transformation of both benzyl alcohol and benzoic acid into benzaldehyde. selleckchem Benzaldehyde was then converted into 4-methoxybenzaldehyde via hydroxylation and subsequent methylation of the 4-C position. The resulting 4-methoxybenzaldehyde was then hydroxylated in the 3-C position followed by methylation into 3,4-dimethoxybenzaldehyde. Based on these findings, a novel metabolic scheme for the biosynthesis of benzylic derivatives in I. resinosum was proposed. The knowledge of the biosynthetic pathway was utilized to produce 4-hydroxy-3-methoxybenzaldehyde (vanillin) from 4-hydroxy-3-methoxybenzoic acid (vanillic acid).